chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117516826117516827CG43GENIChomozygous115847407
7117517206117517218GGGGGTGGAGGC17GENIChomozygous128510589
7117518660117518662AC16GENIChomozygous128510591
7117520169117520170AG41GENIChomozygous115847419
7117521251117521252A26GENIChomozygous128510593
7117521513117521514GC57GENIChomozygous115847421
7117521820117521821GA44GENIChomozygous115847423
7117523204117523205CT42GENIChomozygous115847427
7117526206117526207GA65GENIChomozygous115847431
7117526958117526959TC56GENIChomozygous115847439
7117529191117529192TC49GENIChomozygous115847447
7117529849117529850GT46GENIChomozygous115847451
7117531131117531132TC43GENIChomozygous116302211
7117525827117525828GA57GENICpossibly homozygous116302207
7117525890117525891TC66GENIChomozygous116302208
7117527901117527902GA59GENIChomozygous116302209
7117530810117530811GA55GENIChomozygous116302210
7117531373117531373T48GENICpossibly homozygous131024022
7117533052117533053TC45GENIChomozygous116302212
7117533213117533214CA49GENIChomozygous116302213
7117533357117533358GA59GENIChomozygous115847453
7117534992117535003CATTAATGGGA31GENIChomozygous131024023
7117535124117535125CG41GENIChomozygous116302217
7117535432117535433TC54GENIChomozygous116302218
7117535694117535695GA47GENIChomozygous116302219
7117536968117536969CT59GENICpossibly homozygous116302220
7117537439117537440GA46GENIChomozygous115847457
7117537524117537525CA57GENIChomozygous116302221